EP2787877B1 - Method for combining a plurality of eye images into a plenoptic multifocal image - Google Patents
Method for combining a plurality of eye images into a plenoptic multifocal image Download PDFInfo
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- EP2787877B1 EP2787877B1 EP12855019.1A EP12855019A EP2787877B1 EP 2787877 B1 EP2787877 B1 EP 2787877B1 EP 12855019 A EP12855019 A EP 12855019A EP 2787877 B1 EP2787877 B1 EP 2787877B1
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- A61B3/00—Apparatus for testing the eyes; Instruments for examining the eyes
- A61B3/10—Objective types, i.e. instruments for examining the eyes independent of the patients' perceptions or reactions
- A61B3/12—Objective types, i.e. instruments for examining the eyes independent of the patients' perceptions or reactions for looking at the eye fundus, e.g. ophthalmoscopes
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Definitions
- the present invention is a method for combining a plurality of eye images. More specifically, the present invention is a method for combining a plurality of eye images into a multifocal image.
- Imaging of an eye is typically done with one or more slit lamps, one or more ophthalmoscopes, one or more fundus cameras, one or more scanning laser ophthalmoscopes or SLO's and one or more wide field eye imaging devices that typically acquire a single image. Even when movies or multiple images are acquired they are often at a specific focal plane. When retinal images are shot with different focus and alignment, it is often up to an observer to view multiple images to combine a composite in their mind of the focus regions. While some of these devices allow control of focus, it is difficult to obtain a well-focused image throughout the thickness of a retina or other ocular region. Additionally, there are optical aberrations that can be caused by the eye imaging device that can cause regions to be out of focus. Alignment of the eye imaging device to a patient's eye also can affect overall clarity of regions of images.
- US 2011/234977 discloses to create a multi-focal plenoptic image by aligning images. It determines a central focus of images from different focal planes and aligns them using the respective central focus.
- US 2010/225014 discloses to obtain a composite corneal map from individual imaging fields at different corneal depths.
- the present invention is a method for combining a plurality of eye images. More specifically, the present invention is a method for combining a plurality of eye images into multifocal image
- the invention is defined in the claims.
- the present invention can be utilized in a variety of different operating modalities and in combination with a number of different devices including one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, one or more fundus cameras, one or more ultra-wide field scanning or OPTOS ® wide-field devices, hand-held retinal imaging devices, one or more direct ophthalmoscopes, one or more indirect ophthalmoscopes, one or more scanning laser ophthalmoscopes or one or more generic microscopes, one or more endoscopic probes or one or more optical heads (similar to a fundus camera) attached to a separate chinrest-joystick assembly.
- Each of these modalities and devices allows for registration of one or more image data sets and subsequent image processing to obtain high-frequency in-focus, well-exposed regions from each image data set, combined into a single image or a plenoptic multifocal image, or movie image that allows the user to step through select regions to be viewed that are in focus.
- the one or more image data sets are registered using image processing algorithms on a computer.
- One or more control points to determine the amount of registration may be manually set by human observation or automatically calculated by an algorithm.
- the present invention utilizes the following image processing steps.
- the overall method will correct for translation, rotation, perspective changes and intra-frame warping.
- Third, from the gradient information identify the one or more in-focus regions with a highest magnitude.
- the images can be combined in a number of ways, for example by taking the most in-focus point for each area of the image, or by averaging multiple in-focus regions to improve the signal-to-noise ratio.
- the present invention differs from traditional eye imaging methods that do not account for visualization of multiple in-focus regions of the retina or other ocular region.
- the present invention solves this problem through creating an image registration in combination with image analysis and image processing to yield a plurality of high quality focused plenoptic multifocal images and movies. By creating these multiple images, overall resolution and image quality is greatly improved.
- the present invention can also be utilized with or without discreet focus control.
- An object of the present invention is to provide a method for combining a plurality of eye images into a plenoptic multifocal image that can be utilized in combination with one or more eye imaging modalities including but not limited to color fundus imaging, anterior segment imaging, cornea and lens imaging, fluorescein angiography, Indocyanine green or ICG angiography, curcumin fluorescence imaging, autofluorescence, discreet wavelength imaging, red-free imaging, hyper and multi-spectral imaging and optical coherence tomography.
- eye imaging modalities including but not limited to color fundus imaging, anterior segment imaging, cornea and lens imaging, fluorescein angiography, Indocyanine green or ICG angiography, curcumin fluorescence imaging, autofluorescence, discreet wavelength imaging, red-free imaging, hyper and multi-spectral imaging and optical coherence tomography.
- Another object of the present invention is to provide a method for combining a plurality of eye images into a plenoptic multifocal image with improved resolution, improved focus and increased image quality than a traditional photographic ocular image.
- FIG. 1 illustrates a photographic ocular image 100, in accordance with one embodiment of the present invention.
- the photographic ocular image 100 is generated by one or more traditional eye imaging modalities or devices such as one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, optical coherence tomography or OCT, optical imaging at specific wavelengths, multispectral imaging, hyper spectral imaging, autofluorescence imaging, confocal retinal imaging, scanning laser ophthalmoscopy, one or more adaptive optics devices, one or more polarization orientation specific devices, one or more fundus cameras, one or more hand held imagers, one or more direct and indirect ophthalmoscopes, fluorescein angiography, ICG angiography, curcumin fluorescence imaging, autofluorescence and other suitable traditional eye imaging modalities and devices.
- traditional eye imaging modalities or devices such as one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, optical coherence tomography or OCT, optical imaging at specific wavelengths, multispectral imaging, hyper spectral imaging, autofluorescence imaging, confocal retina
- the photographic ocular image 100 generated in FIG. 1 is a fundus autofluorescence image but can be any photographic ocular image generated by one or more traditional eye imaging modalities or devices such as one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, optical coherence tomography or OCT, optical imaging at specific wavelengths, multispectral imaging, hyper-spectral imaging, autofluorescence imaging, confocal retinal imaging, scanning laser ophthalmoscopy, one or more adaptive optics devices, one or more polarization orientation specific devices, one or more fundus cameras, one or more hand held imagers, one or more direct and indirect ophthalmoscopes, fluorescein angiography, ICG angiography or curcumin fluorescence imaging, or autofluorescence.
- traditional eye imaging modalities or devices such as one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, optical coherence tomography or OCT, optical imaging at specific wavelengths, multispectral imaging, hyper-spectral
- the images are automatically aligned by computer. This is achieved by taking each frame and comparing it to a reference. First the overall translation, rotation and perspective changes are corrected. The amount of correction is determined by identifying the shift between various common features in the images utilizing feature detection or cross-correlation. Then the images are broken into small sub-regions and the shift between corresponding sub-regions is determined. The shifts for each subregion are used to warp each part of the image in a continuous manner such that features in the resulting image are aligned with the reference image. The aligned image may also be combined with the reference image to produce a more accurate reference for subsequent use with other frames. The eye images are combined by averaging multiple in-focus regions to improve a signal-to-noise ratio or SNR.
- the SNR can be defined as 20 * log10 (standard_deviation_image / standard_deviation_noise) with units of dB.
- the photographic ocular image 100 illustrated in FIG. 1 has an estimated SNR of 10 dB.
- FIG. 2 illustrates a photographic image 200 of a plurality of eye images 210 that are formed into a plenoptic multifocal image 220, in accordance with one embodiment of the present invention.
- the photographic image 200 of the eye images 210 into the plenoptic multifocal image 220 illustrated and described in FIG. 2 and its description is similar to the photographic ocular image 100 illustrated and described in FIG. 1 and its description.
- the photographic image 200 of the eye images 210 into the plenoptic multifocal image 220 illustrated and described in FIG. 2 and its description has been generated by a method for combining a plurality of eye images into a plenoptic multifocal image ( FIG. 3 and FIG. 4 , 300, 400).
- the method for combining a plurality of eye images into a plenoptic multifocal image FIG. 3 and FIG.
- the photographic ocular image 200 illustrated in FIG. 2 is a 15 frame, aligned, averaged and enhanced image with an estimated SNR of 42 dB.
- the method for combining a plurality of eye images into a plenoptic multifocal image can be for imaging eye documentation of an eye's anatomy and/or detection of eye pathology.
- the method for combining a plurality of eye images into a plenoptic multifocal image can be utilized for imaging an anterior segment, a posterior segment and a substructure of an eye as seen in OCT.
- One feature of the method for combining a plurality of eye images into a plenoptic multifocal image is an automated registration of images and then subsequent image processing to identify regions that are well-focused, evenly illuminated and to obtain high frequency image information (e.g.
- An algorithm is also capable of eliminating areas of the images that are poorly focused, contain other optical aberrations and/or are not well illuminated.
- the well-focused regions are identified from the regions with the largest calculated gradient magnitude.
- the evenly illuminated regions are determined by over-smoothing the image and comparing the average intensity with the overall image intensity. Those regions significantly below the average are considered poorly illuminated and should be excluded from analysis.
- High frequency image information is calculated by removing one or more low frequency image components and by smoothing and suppressing one or more random noise variations.
- a multi-scale gradient calculation is one method of obtaining high frequency image information.
- the high frequency image information is an indication of when the image is in-focus. Poorly focused images or regions will have lower magnitude gradients compared to an in-focus frame. These parts will be excluded from the analysis.
- the method for combining a plurality of eye images into a plenoptic multifocal image can be applied to new eye imaging devices that specifically step the focus and/or existing devices that may or may not require the user to change the focus.
- the method for combining a plurality of eye images into a plenoptic multifocal image can also be applied by deliberately stepping the focus of a device to generate an image set.
- the method for combining a plurality of eye images into a plenoptic multifocal image utilizes a variety of eye imaging modalities (alone or in combination) including but not limited to one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, OCT, optical imaging at specific wavelengths, multispectral imaging, hyper spectral imaging, autofluorescence imaging, confocal retinal imaging, scanning laser ophthalmoscopy, adaptive optics imaging, polarization orientation specific imaging, one or more fundus cameras, one or more hand held imagers, one or more direct ophthalmoscopes and one or more indirect ophthalmoscopes, fluorescein angiography, ICG angiography, curcumin fluorescence imaging, autofluorescence and other eye imaging modalities.
- eye imaging modalities including but not limited to one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, OCT, optical imaging at specific wavelengths, multispectral imaging, hyper spectral imaging, autofluor
- Image data sets are acquired either with random or deliberate focus and exposure control. Image data sets are automatically registered with sub-pixel accuracy. Image processing is performed on data sets to identify clear, well-exposed portions of data sets and eliminate relatively poorly defined and/or dark data sets or other aberrations that degrade imaging quality. Good or well-suited image data is then recombined into a single image that is plenoptic or in focus at multiple depths and/or a movie file is created that allows the user to step through a focus stack or select a region that they want to view that is in focus.
- the term "step through selected regions” is defined as to change the focal position of interest. The term step through selected regions is similar to scrolling through frames in a movie. Stepping through a focus stack involves changing the viewed image from a collected sequence of frames where the focus is changed between each frame. A multi-focus sequence of images can be formed by changing the focus between each collected frame. Each image is then an optical-slice of the object.
- a micro-lens array can be used to collect the light-field of a scene, which allows the focus to be changed post-acquisition, and thus a multi-focus stack can be calculated.
- the image is collected using one or more high density camera sensors (e.g. one or more CCD or CMOS sensors) or one or more point and line scanning devices.
- the resulting image stack will have a lower resolution compared to the source images when using a micro-lens array.
- the multiple image planes contain the in-focus structures from the corresponding focal plane in the specimen. Out-of-focus information from surrounding structures will also contaminate the image collected.
- the method for combining a plurality of eye images into a plenoptic multifocal image generates an image data set obtained from existing eye imaging devices.
- the method for combining a plurality of eye images into a plenoptic multifocal image generates a plurality of image data sets obtained from new eye imaging devices specifically designed to create images that are in focus at various depths either through stepping focus or a multi-element microlens that is placed over a sensor that contains information from multiple image planes.
- the method for combining a plurality of eye images into a plenoptic multifocal image is applied to one or more OCT data sets to obtain one or more relatively clear comprehensive OCT data sets.
- FIG. 3 illustrates a flowchart of a first method for combining a plurality of eye images into a plenoptic multifocal image 300, in accordance with one embodiment of the present invention.
- the first method 300 for combining a plurality of eye images into a plenoptic multifocal image includes the steps of registering the eye images with a plurality of frames into one or more eye image sets with a processor and a memory system 310, aligning each of the eye images in each of the one or more image sets with a selected reference that resides on the memory system with the processor 320, determining one or more in-focus regions of the eye images by calculating one or more gradient images while ignoring noise and other imaging artifacts 330, identifying the one or more in-focus regions with highest resolution from the one or more gradient images 340 and selecting one or more corresponding in-focus intensities from the frames to combine into the plenoptic multifocal image with a higher resolution than the eye images, the frames and the one or more eye image sets 350.
- the registering step 310 is controlled by a predetermined quantity of control points, where the predetermined quantity of control points is manually set by user observation or is automatically calculated by the processor.
- the processor utilizes an image processing algorithm to automatically calculate the predetermined quantity of control points.
- the eye images, the frames, the image sets and the predetermined quantity of control points reside on the memory system.
- the aligning step 320 includes that the eye images are collected using one or more high density camera sensors.
- the one or more high density camera sensors are one or more charge coupled device sensors or CCD sensors or the one or more high density camera sensors are one or more complementary metal oxide semiconductor sensors or CMOS sensors, or one or more point and line scanning devices.
- the determining step 330 includes that the eye images are combined by taking the one or more in-focus points with highest resolution from each of the eye images.
- the identifying step 340 includes that the eye images are combined by taking the most in-focus point in each of the eye images.
- the eye images are combined by averaging multiple in-focus regions to improve a signal-to-noise ratio or SNR.
- the plenoptic multifocal image is generated by one or more traditional eye imaging modalities or devices selected from the group of one or more slit lamp mounted cameras, one or more slit lamp integrated cameras, optical coherence tomography, optical imaging at specific wavelengths, multispectral imaging, hyper spectral imaging, autofluorescence imaging, confocal retinal imaging, scanning laser ophthalmoscopy, one or more adaptive optics devices, one or more polarization orientation specific devices, one or more fundus cameras, one or more hand held imagers, one or more direct and indirect ophthalmoscopes, fluorescein angiography, ICG angiography and curcumin fluorescence imaging, or autofluorescence.
- the selecting step 350 identifies the one or more in-focus regions that are well-focused, evenly illuminated and obtains high frequency image information to recombine the processed images into the plenoptic multifocal image.
- the plurality of eye images may be a larger montage image made of a plurality of individual optimized frames.
- the high frequency image information is calculated by removing one or more low frequency image components and by smoothing and suppressing one or more random noise variations.
- the method 300 is applied by stepping focus to generate the one or more eye image sets. The method 300 also creates the images that are in focus at various depths through the stepping focus.
- FIG. 4 illustrates a flowchart of a second method for combining a plurality of eye images into a plenoptic multifocal image 400, in accordance with one embodiment of the present invention.
- the second method 400 includes the steps of registering a plurality of eye images with a plurality of frames into one or more eye image sets with a processor and a memory system, the registering is controlled by a predetermined quantity of control points, the eye images are collected using one or more high density camera sensors and the eye images are combined by taking the one or more in-focus points with highest resolution from one or more evenly illuminated sections from each of the eye images 410, aligning each of the eye images in each of the one or more image sets with a selected reference that resides on the memory system with the processor 420, determining one or more in-focus regions of the eye images by calculating one or more gradient images while ignoring noise and other imaging artifacts, the one or more in-focus regions that are well-focused, evenly illuminated and obtain high frequency image information recombine the processed images into the plenoptic multifocal image 430, identifying the one or more in-focus regions with highest resolution from the one or more gradient images 440 and selecting one or more corresponding in-focus intensities from the frames to
- the second method for combining a plurality of eye images into a plenoptic multifocal image 400 illustrated and described in FIG. 4 and its description is similar to the first method for combining a plurality of eye images into a plenoptic multifocal image 300 illustrated and described in FIG. 3 and its description.
- the second method for combining a plurality of eye images into a plenoptic multifocal image 400 includes the one or more high density camera sensors or one or more point and line scanning devices. Additionally, the one or more in-focus regions are well-focused, evenly illuminated and obtain high frequency image information using a frequency domain filter or a Weiner filter and recombine the processed images into the one or more images.
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Applications Claiming Priority (2)
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US201161568851P | 2011-12-09 | 2011-12-09 | |
PCT/US2012/068646 WO2013086473A1 (en) | 2011-12-09 | 2012-12-08 | Method for combining a plurality of eye images into a plenoptic multifocal image |
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EP2787877A1 EP2787877A1 (en) | 2014-10-15 |
EP2787877A4 EP2787877A4 (en) | 2015-08-12 |
EP2787877B1 true EP2787877B1 (en) | 2022-04-06 |
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US (1) | US8814362B2 (ja) |
EP (1) | EP2787877B1 (ja) |
JP (1) | JP2015506730A (ja) |
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MX (1) | MX337930B (ja) |
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Families Citing this family (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5822485B2 (ja) * | 2011-02-25 | 2015-11-24 | キヤノン株式会社 | 画像処理装置、画像処理方法、画像処理システム、slo装置、およびプログラム |
US8998411B2 (en) | 2011-07-08 | 2015-04-07 | Carl Zeiss Meditec, Inc. | Light field camera for fundus photography |
EP3922270A1 (en) | 2011-12-09 | 2021-12-15 | Regents of the University of Minnesota | Hyperspectral imaging for early detection of alzheimer's disease |
US9016862B2 (en) * | 2012-05-10 | 2015-04-28 | Sonomed Ip Holdings, Inc. | Multimodality correlation of optical coherence tomography using secondary reference images |
US9456746B2 (en) | 2013-03-15 | 2016-10-04 | Carl Zeiss Meditec, Inc. | Systems and methods for broad line fundus imaging |
US9215977B2 (en) * | 2013-03-25 | 2015-12-22 | David KOHN BITRAN | Portable device for indirect ophthalmology |
US9237847B2 (en) | 2014-02-11 | 2016-01-19 | Welch Allyn, Inc. | Ophthalmoscope device |
US9211064B2 (en) | 2014-02-11 | 2015-12-15 | Welch Allyn, Inc. | Fundus imaging system |
WO2015162098A1 (en) | 2014-04-24 | 2015-10-29 | Carl Zeiss Meditec, Inc. | Functional vision testing using light field displays |
WO2016033590A1 (en) | 2014-08-31 | 2016-03-03 | Berestka John | Systems and methods for analyzing the eye |
CN104287692B (zh) * | 2014-11-06 | 2017-12-19 | 苏州微清医疗器械有限公司 | 一种眼底照相装置 |
US10582852B2 (en) | 2015-02-05 | 2020-03-10 | Carl Zeiss Meditec Ag | Method and apparatus for reducing scattered light in broad-line fundus imaging |
US11045088B2 (en) | 2015-02-27 | 2021-06-29 | Welch Allyn, Inc. | Through focus retinal image capturing |
US10799115B2 (en) | 2015-02-27 | 2020-10-13 | Welch Allyn, Inc. | Through focus retinal image capturing |
US9967535B2 (en) * | 2015-04-17 | 2018-05-08 | Light Labs Inc. | Methods and apparatus for reducing noise in images |
US10136804B2 (en) | 2015-07-24 | 2018-11-27 | Welch Allyn, Inc. | Automatic fundus image capture system |
US10506165B2 (en) | 2015-10-29 | 2019-12-10 | Welch Allyn, Inc. | Concussion screening system |
US10772495B2 (en) | 2015-11-02 | 2020-09-15 | Welch Allyn, Inc. | Retinal image capturing |
US10003738B2 (en) | 2015-12-18 | 2018-06-19 | Light Labs Inc. | Methods and apparatus for detecting and/or indicating a blocked sensor or camera module |
US10413179B2 (en) | 2016-01-07 | 2019-09-17 | Welch Allyn, Inc. | Infrared fundus imaging system |
AU2017229876A1 (en) | 2016-03-10 | 2018-11-01 | Regents Of The University Of Minnesota | Spectral-spatial imaging device |
US10602926B2 (en) | 2016-09-29 | 2020-03-31 | Welch Allyn, Inc. | Through focus retinal image capturing |
US10285589B2 (en) | 2016-09-30 | 2019-05-14 | Welch Allyn, Inc. | Fundus image capture system |
JP7308144B2 (ja) * | 2016-10-13 | 2023-07-13 | トランスレイタム メディカス インコーポレイテッド | 眼疾患の検出のためのシステム及び方法 |
CN111565624A (zh) | 2017-11-27 | 2020-08-21 | 雷蒂斯派克股份有限公司 | 用于阿尔茨海默氏病病理的高光谱图像指导的raman眼科成像仪 |
US11096574B2 (en) | 2018-05-24 | 2021-08-24 | Welch Allyn, Inc. | Retinal image capturing |
CN112867433B (zh) | 2018-09-28 | 2024-07-23 | 卡尔蔡司医疗技术公司 | 具有用于对准辅助的集成瞳孔相机的低成本眼底成像器 |
KR102250688B1 (ko) * | 2018-12-13 | 2021-05-12 | 서울대학교병원 | 안저 영상과 형광안저혈관조영 영상의 정합을 이용한 자동 혈관 분할 장치 및 방법 |
US12079958B2 (en) * | 2019-04-19 | 2024-09-03 | Nidek Co., Ltd. | Method of and apparatus for creating an all-in-focus image of a portion of an iridocorneal angle of an eye |
JP7346594B2 (ja) * | 2019-05-24 | 2023-09-19 | オッポ広東移動通信有限公司 | ユーザ機器及び斜視補正方法 |
WO2022063806A1 (de) * | 2020-09-22 | 2022-03-31 | K|Lens Gmbh | Verfahren zur erstellung einer bildaufzeichnung |
CN116883461B (zh) * | 2023-05-18 | 2024-03-01 | 珠海移科智能科技有限公司 | 一种用于获取清晰文档图像的方法及其终端装置 |
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JP3956584B2 (ja) * | 2000-06-02 | 2007-08-08 | 株式会社日立製作所 | 全焦点画像合成方法及び装置 |
JP4901230B2 (ja) * | 2006-02-08 | 2012-03-21 | 興和株式会社 | 撮像システム |
JP4863207B2 (ja) * | 2006-07-04 | 2012-01-25 | 国立大学法人愛媛大学 | 眼科装置 |
US7854510B2 (en) * | 2008-10-16 | 2010-12-21 | Steven Roger Verdooner | Apparatus and method for imaging the eye |
AU2011232625B2 (en) * | 2010-03-23 | 2014-01-16 | Neurovision Imaging, Inc. | Apparatus and method for imaging an eye |
CN102008289A (zh) * | 2010-12-08 | 2011-04-13 | 苏州六六宏医疗器械有限公司 | 基于自动寻优算法的像差补偿眼底显微镜 |
JP2012213555A (ja) * | 2011-04-01 | 2012-11-08 | Topcon Corp | 眼底撮影装置 |
WO2013067468A1 (en) * | 2011-11-04 | 2013-05-10 | Josh Hogan | Improved correlation of non-invasively acquired signals |
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